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Corydalis bungeana

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64401390b9698752915261
Scientific name Corydalis bungeana
Authority Turcz.
First published in Bull. Soc. Imp. Naturalistes Moscou 13: 62 (1840)

Description Top

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Synonyms Top

Scientific name Authority First published in
Capnoides bungeana Kuntze Revis. Gen. Pl. 1: 14 (1891)
Corydalis racemosa Bunge Enum. Pl. China Bor. [A.A. von Bunge] 5. 1833 [Mar 1833]
Corydalis bungeana var. odontopetala Hemsl. J. Linn. Soc., Bot. 23: 36 1886

Common names Top

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Language Common/alternative name
Chinese 苦丁
Chinese 苦地丁
Chinese 萨巴乐干纳
Chinese 地丁草
Chinese 地丁草（布氏紫堇、紫堇）
Chinese 本氏紫堇
Chinese 哈达存额布斯
Chinese 好如海其格
Chinese 布氏地丁
Chinese 彭氏紫堇
Chinese 紫堇
Chinese 紫花地丁

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
      • Sakhalin

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000622135
UNII 732H9A883V
Tropicos 24000394
KEW urn:lsid:ipni.org:names:672108-1
The Plant List kew-2738529
Open Tree Of Life 5263529
Observations.org 116732
NCBI Taxonomy 1238147
IPNI 672108-1
GBIF 5531124
EPPO COYBU
Elurikkus 538588

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
From Plant to Chemistry: Sources of Active Opioid Antinociceptive Principles for Medicinal Chemistry and Drug Design Turnaturi R, Piana S, Spoto S, Costanzo G, Reina L, Pasquinucci L, Parenti C Molecules 14-Oct-2023
PMCID:PMC10609244
doi:10.3390/molecules28207089
PMID:37894567
A study on the effect of natural products against the transmission of B.1.1.529 Omicron Alkafaas SS, Abdallah AM, Hussien AM, Bedair H, Abdo M, Ghosh S, Elkafas SS, Apollon W, Saki M, Loutfy SA, Onyeaka H, Hessien M Virol J 25-Aug-2023
PMCID:PMC10464336
doi:10.1186/s12985-023-02160-6
PMID:37626376
Dandelion (Taraxacum Genus): A Review of Chemical Constituents and Pharmacological Effects Fan M, Zhang X, Song H, Zhang Y Molecules 27-Jun-2023
PMCID:PMC10343869
doi:10.3390/molecules28135022
PMID:37446683
Alkaloids as Natural NRF2 Inhibitors: Chemoprevention and Cytotoxic Action in Cancer Gjorgieva Ackova D, Maksimova V, Smilkov K, Buttari B, Arese M, Saso L Pharmaceuticals (Basel) 07-Jun-2023
PMCID:PMC10300961
doi:10.3390/ph16060850
PMID:37375797
Natural compounds protect against the pathogenesis of osteoarthritis by mediating the NRF2/ARE signaling Wu Z, Yang Z, Liu L, Xiao Y Front Pharmacol 30-May-2023
PMCID:PMC10266108
doi:10.3389/fphar.2023.1188215
PMID:37324450
Maternal traditional Chinese medicine exposure and risk of congenital malformations: a multicenter prospective cohort study Peng T, Yin L, Xiong Y, Xie F, Ji C, Yang Z, Pan Q, Li M, Deng X, Dong J, Wu J Acta Obstet Gynecol Scand 19-Apr-2023
PMCID:PMC10201976
doi:10.1111/aogs.14553
PMID:37073619
Metabolomic Characteristics of Cecum Contents in High-Fat-Diet-Induced Obese Mice Intervened with Different Fibers Zhang Q, Cheng J, Jiang X, Tang J, Zhu C, Chen H, Laghi L Foods 26-Mar-2023
PMCID:PMC10093315
doi:10.3390/foods12071403
PMID:37048225
Therapeutic drug combinations against COVID-19 obtained by employing a collaborative filtering method Yao R, Yang F, Liu J, Jiao Q, Yu H, Nie X, Li H, Wang X, Xue F Heliyon 25-Feb-2023
PMCID:PMC9958039
doi:10.1016/j.heliyon.2023.e14023
PMID:36873530
Protective effects of Pudilan Tablets against osteoarthritis in mice induced by monosodium iodoacetate Fang Z, Li X, Lei S, Feng S, Zhou C, Tong X, Han R Sci Rep 16-Feb-2023
PMCID:PMC9935914
doi:10.1038/s41598-023-29976-0
PMID:36797333
Targeted activation of Nrf2/HO‐1 pathway by Corynoline alleviates osteoporosis development Xu T, Lin B, Huang C, Sun J, Tan K, Ma R, Huang Y, Weng S, Fang W, Chen W, Bai B Food Sci Nutr 24-Jan-2023
PMCID:PMC10084958
doi:10.1002/fsn3.3239
PMID:37051369
Gut microbiome sheds light on the development and treatment of abdominal aortic aneurysm Ling X, Jie W, Qin X, Zhang S, Shi K, Li T, Guo J Front Cardiovasc Med 25-Nov-2022
PMCID:PMC9732037
doi:10.3389/fcvm.2022.1063683
PMID:36505348
The protective effect of natural medicines against excessive inflammation and oxidative stress in acute lung injury by regulating the Nrf2 signaling pathway Luan R, Ding D, Yang J Front Pharmacol 16-Nov-2022
PMCID:PMC9709415
doi:10.3389/fphar.2022.1039022
PMID:36467050
Antiviral effects of phytochemicals against severe acute respiratory syndrome coronavirus 2 and their mechanisms of action: A review Jantan I, Arshad L, Septama AW, Haque MA, Mohamed‐Hussein Z, Govender NT Phytother Res 07-Nov-2022
PMCID:PMC9878073
doi:10.1002/ptr.7671
PMID:36343627
A mini-review on co-supplementation of probiotics and medicinal herbs: Application in aquaculture Wei LS, Goh KW, Abdul Hamid NK, Abdul Kari Z, Wee W, Van Doan H Front Vet Sci 02-Nov-2022
PMCID:PMC9666728
doi:10.3389/fvets.2022.869564
PMID:36406063
Antimicrobial activities and mechanisms of extract and components of herbs in East Asia Liang J, Huang X, Ma G RSC Adv 12-Oct-2022
PMCID:PMC9554739
doi:10.1039/d2ra02389j
PMID:36320733

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
Isoboldine 133323 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown https://doi.org/10.1055/S-2006-962761
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
Dihydrosanguinarine 124069 Click to see CN1CC2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C=C4)OCO6 333.30 unknown https://doi.org/10.1055/S-2006-962761
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Hexahydrobenzophenanthridine alkaloids
(11alpha)-13-Methylchelidonine 185284 Click to see CC12C(CC3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O 367.40 unknown https://doi.org/10.1016/0031-9422(88)83149-2
(12S)-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-12-ol 5316101 Click to see CC12C(CC3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O 367.40 unknown https://doi.org/10.1055/S-2006-962761
(1S,12R,13R)-13,24-dimethyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-2,4(8),9,14(22),15,17(21)-hexaen-12-ol 12304073 Click to see CC12C(CC3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O 367.40 unknown https://doi.org/10.1016/0031-9422(88)83149-2
12-Hydroxycorynoline 101806253 Click to see CC12C(C(C3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O)O 383.40 unknown https://doi.org/10.1055/S-2006-962761
24,25-Dimethyl-5,7,13,17,19-pentaoxa-25-azaheptacyclo[12.10.1.02,10.04,8.012,24.015,23.016,20]pentacosa-2,4(8),9,15(23),16(20),21-hexaene 5316102 Click to see CC12C3CC4=CC5=C(C=C4C1N(C(O3)C6=C2C=CC7=C6OCO7)C)OCO5 365.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268814/
Acetylcorynoline 177015 Click to see CC(=O)OC1CC2=CC3=C(C=C2C4C1(C5=C(CN4C)C6=C(C=C5)OCO6)C)OCO3 409.40 unknown https://doi.org/10.1055/S-2006-962761
Corynoline 177014 Click to see CC12C(CC3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O 367.40 unknown https://doi.org/10.1055/S-2006-962761
> Alkaloids and derivatives / Phthalide isoquinolines
Bicuculline 10237 Click to see CN1CCC2=CC3=C(C=C2C1C4C5=C(C6=C(C=C5)OCO6)C(=O)O4)OCO3 367.40 unknown https://doi.org/10.1055/S-2006-962761
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(13aR)-3,10-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-2,9-diol 1152279 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O 327.40 unknown https://doi.org/10.1055/S-2006-962761
Chelianthifoline 5117621 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)O 325.40 unknown https://doi.org/10.1055/S-2006-962761
Scoulerine 22955 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O 327.40 unknown https://doi.org/10.1055/S-2006-962761
> Alkaloids and derivatives / Protopine alkaloids
Corycavine 276145 Click to see CC1C2=C(CN(CCC3=CC4=C(C=C3C1=O)OCO4)C)C5=C(C=C2)OCO5 367.40 unknown https://doi.org/10.1055/S-2006-962761
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
https://doi.org/10.1055/S-2006-962761
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(R)-Juziphine 14526072 Click to see CN1CCC2=C(C1CC3=CC=C(C=C3)O)C(=C(C=C2)OC)O 299.40 unknown https://doi.org/10.1055/S-2006-962761
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
[1,3]Dioxolo[4,5-g]isoquinolin-5(6H)-one 12997610 Click to see C1OC2=C(O1)C=C3C(=C2)C=CNC3=O 189.17 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
6,7-Methylenedioxy-2-(6-acetyl-2,3-methylene-dioxybenzyl)-1(2h)-isoquinolinone 12997611 Click to see CC(=O)C1=C(C2=C(C=C1)OCO2)CN3C=CC4=CC5=C(C=C4C3=O)OCO5 365.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(13-Methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-1(24),2,4(8),9,14(22),15,17(21)-heptaen-12-yl) acetate 163084588 Click to see CC(=O)OC1CC2=CC3=C(C=C2C4=NCC5=C(C14C)C=CC6=C5OCO6)OCO3 393.40 unknown https://doi.org/10.1055/S-2006-962761
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 163195618 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 596.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl]Oxy-Chromen-4-one 12304323 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
3-[(6-O-alpha-L-arabinopyranosyl-beta-D-glucopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one 13887800 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 596.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162946489 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 580.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 14334890 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 580.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
6''-O-L-Arabinopyranosylastragalin 45359554 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 580.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
Peltatoside 5484066 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 596.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
Vitamin P 5293655 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 12314848 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 163195229 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O)O)O 758.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 101362013 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O)O)O 758.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 162960876 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O)O)O 758.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
5-Hydroxy-2-(4-hydroxyphenyl)-3,7-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]chromen-4-one 13647408 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
5-hydroxy-2-(4-hydroxyphenyl)-7-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 163189273 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O 742.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 101362012 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O 742.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
5-Hydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 162898016 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O 742.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
acs.jmedchem.1c00409_ST.719 13345442 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
Kaempferol 3,7-diglucoside 6325460 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
Quercetin 3-rutinoside 7-galactoside 13942388 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O)O)O 772.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
Quercetin 3-rutinoside-7-glucoside 10190763 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O)O)O 772.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
Quercetin 3,7-diglucoside 10121947 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009
Quercetin 7-O-glucoside 5381351 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.09.009

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